Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1085307766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome15
Position92942998
GeneCHD2
is asnp
is mentioned by
dbSNPrs1085307766
dbSNP (old)rs1085307766
ClinGenrs1085307766
ebirs1085307766
HLIrs1085307766
Exacrs1085307766
Gnomadrs1085307766
Varsomers1085307766
Maprs1085307766
PheGenIrs1085307766
Biobankrs1085307766
1000 genomesrs1085307766
hgdprs1085307766
ensemblrs1085307766
gopubmedrs1085307766
geneviewrs1085307766
scholarrs1085307766
googlers1085307766
pharmgkbrs1085307766
gwascentralrs1085307766
openSNPrs1085307766
23andMers1085307766
23andMe allrs1085307766
SNPshotrs1085307766
SNPdbers1085307766
MSV3drs1085307766
GWAS Ctlgrs1085307766
Max Magnitude0
ClinVar
Risk rs1085307766(T;T)
Alt rs1085307766(T;T)
Reference Rs1085307766(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93486228C>T
CLNSRC
CLNACC RCV000488989.1,